Effect of Dyslipidemia Therapy on Creatinine Kinase Activity Level in Patients with Heart Disease

Authors

  • Waode Dila Sulistian Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya
  • Muhamad Ro'biul Fuadi Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya/ Laboratorium of Clinical Pathology, Faculty of Medicine, Airlangga University Hospital, Surabaya
  • Soebagijo Poegoeh Edijanto Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya
  • Mochammad Yusuf Department of Cardiology and Vascular Medicine, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya

DOI:

https://doi.org/10.24293/ijcpml.v27i2.1631

Keywords:

Dyslipidemia, Atorvastatin, Simvastatin, creatinine kinase, enzymatic methods

Abstract

Cardiovascular disease remains a significant health problem in the Asia Pacific region. Several studies have found that dyslipidemia is a cause of morbidity and mortality and requires high medical costs. Dyslipidemia is a risk factor for atherosclerosis. The most widely used therapy for dyslipidemia is statins. Statins often cause muscle disorders such as myalgia, myopathy, and rhabdomyolysis, which can cause death. A prospective cohort study design was carried out at Airlangga University Hospital, Surabaya, from April to November 2019. A total of 26 sample pairs containing 13 samples were treated with Atorvastatin, and 13 samples were treated with Simvastatin. The subjects were examined for the creatinine kinase activity level using enzymatic methods. The mean creatinine kinase levels in the atorvastatin group before and after treatment was 105.71 IU/L and 100.03 IU/L, respectively, because the subjects were diagnosed with acute coronary syndromes and blood was collected during acute conditions. Median creatinine kinase levels in the Simvastatin group were 85.5 IU/L before therapy and 118.1 IU/L after therapy, indicating significant differences in creatinine kinase levels before and after treatment. Simvastatin is very susceptible to certain drug interactions that can increase the concentration of statins in the serum. There were differences in levels of creatinine kinase activity before and after Simvastatin therapy but not Atorvastatin.

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Author Biographies

Waode Dila Sulistian, Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya

Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya

Muhamad Ro'biul Fuadi, Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya/ Laboratorium of Clinical Pathology, Faculty of Medicine, Airlangga University Hospital, Surabaya

Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya/ Laboratorium of Clinical Pathology, Faculty of Medicine, Airlangga University Hospital, Surabaya

Soebagijo Poegoeh Edijanto, Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya

Department of Clinical Pathology, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya

Mochammad Yusuf, Department of Cardiology and Vascular Medicine, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya

Department of Cardiology and Vascular Medicine, Faculty of Medicine, Airlangga University/Dr. Soetomo Hospital, Surabaya

References

Moor VJA, Amougou SN, Ombotto S, Ntone F, Wouamba DE, Nonga BN. Dyslipidemia in patients

with a cardiovascular risk and disease at the University Teaching Hospital of Yaoundé, Cameroon.

International Journal of Vascular Medicine, Hindawi Publishing Corporation, 2017; 2017: 1-5.

Lin CF, Chang YH, Chien SC, Lin YH, Yeh HY. Epidemiology of dyslipidemia in the Asia Pacific

Region. International Journal of Gerontology, 2018; 12(1): 2–6.

Carreras ET, Polk DM. Dyslipidemia; Current therapies and guidelines for treatment. US Cardiology Review, 2017; 11(1): 10-5.

Ramkumar S, Raghunath A, Raghunath S. Statin therapy: Review of safety and potential side effects.

Acta Cardiol Sin, 2016; 32(6): 631-639.

Rosenson RS, Baker S, Banach M, Borrow KM, Braun LT, et al. Optimizing cholesterol treatment in patients with muscle complaints. Journal of American College of Cardiology, 2017; 70(10): 1290–1301.

Stroes ES, Thompson PD, Corsini A, Vladutiu GD, Raal FJ, et al. Statin associated muscle symptoms:

Impact on Statin therapy-European atherosclerosis society consensus panel statement on assessment,

etiology, and management. European Heart Journal, 2015; 36: 1012-1022.

Nogueira AA, Strunz CM, Takada JY, Mansur AP. Biochemical markers of muscle damage and high

serum concentration of creatine kinase in patients on statin therapy. Biomarkers in Medicine, 2019; 13: 8.

Muhibbah, Wahid A, Agustina R, Illiandri O. Karakteristik pasien sindrom koroner akut pada pasien rawat inap Ruang Tulip di RSUD Ulin Banjarmasin. Indonesian Journal for Health Sciences, 2019; 3(1): 6–12.

Kawamoto KR, Davis MB, Duvernoy CS. Acute coronary syndromes: Differences in men and women. Curr Atheroscler Rep, 2016; 18: 73.

Nuzzo A, Rossi R, Modena MG. Hypertension alone or related to the metabolic syndrome in post-menopausal women. Expert Review of Cardiovascular Therapy, 2015; 8(11): 1541–1548.

Mirghani HO. Age-related differences in acute coronary syndrome presentation and in-hospital

outcomes: A cross-sectional comparative study. Pan African Medical Journal, 2016; 24(337): 1–5.

Nkoke C, Makoge C, Dzudie A, Mfeukeu LK, Luchuo EB, et al. A predominance of hypertensive heart disease among patients with cardiac disease in Buea, a semi-urban setting, South West Region of Cameroon. BMC Research Notes, BioMed Central, 2017; 10(684): 1–6.

Petrie JR, Guzik TJ, Touyz RM. Diabetes, hypertension, and cardiovascular disease: Clinical insights and vascular mechanisms. Canadian Journal of Cardiology, 2018; 34(5): 575–584.

Zhou M, Liu J, Hao Y, Liu J, Huo Y, et al. Prevalence and in-hospital outcomes of diabetes among patients with acute coronary syndrome in China: Findings from the improving care for cardiovascular disease in China-acute coronary syndrome project. Cardiovasc Diabetol, 2018; (17): 147.

Kjeldsen SE. Hypertension and cardiovascular risk: General aspects. Pharmacological Research, Elsevier Ltd, 2017; 12: 95–99.

Ralapanawa U, Kumarasiri PVR, Jayawickreme KP, Kumarihamy P, Wijeratne Y, et al. Epidemiology and risk factors of patients with types of acute coronary syndrome presenting to a tertiary care hospital in Sri Lanka. BMC Cardiovascular Disorders, 2019; 19(229): 1–9.

Danese E, Montagnana M. An historical approach to the diagnostic biomarkers of acute coronary

syndrome. Annals of Translational Medicine, 2016; 4(8): 1–11.

Morales D, Parker B, Thompson PD. Increases CK level on high doses of Atorvastatin are related to decreases in muscle strength but do not predict myalgia. American Heart Association Journal, 2018; 126(21): 11708.

Wang YC, Hsieh TC, Chou CL, Wu JL, Fang TC. Risks of adverse events following prescription of statins and calcium channel blockers. Medicine (Baltimore), 2016; 95(2): e2487.

Ward NC, Watts GF, Eckel RH. Statin toxicity. Circulation Research, 2019; 124: 328-350.

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Submitted

2020-02-12

Accepted

2020-07-07

Published

2021-04-15

How to Cite

[1]
Sulistian, W.D., Fuadi, M.R., Edijanto, S.P. and Yusuf, M. 2021. Effect of Dyslipidemia Therapy on Creatinine Kinase Activity Level in Patients with Heart Disease. INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY. 27, 2 (Apr. 2021), 132–137. DOI:https://doi.org/10.24293/ijcpml.v27i2.1631.

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